Canonical Allele Identifier: PA2827998661
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133522
ClinVar RCV Id: RCV000120032 RCV000131590 RCV000587624 RCV001153055 RCV003323291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2438Leu
CA013717
NM_001354901.2:c.7313C>T